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FDA 510(k)

P.F.C. CERAMIC HIP HEAD

K-Number: K962248 · 1996-08-29

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1996-08-29
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.F.C. CERAMIC HIP HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1996-08-29 under 510(k) number K962248. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.F.C. CERAMIC HIP HEAD?

P.F.C. CERAMIC HIP HEAD is a medical device that received FDA 510(k) clearance on 1996-08-29. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K962248.

When did P.F.C. CERAMIC HIP HEAD receive FDA 510(k) clearance?

P.F.C. CERAMIC HIP HEAD received FDA 510(k) clearance on 1996-08-29, under 510(k) number K962248.

Who is the listed applicant for P.F.C. CERAMIC HIP HEAD?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P.F.C. CERAMIC HIP HEAD?

The FDA product code for P.F.C. CERAMIC HIP HEAD is LZO.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: LZO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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